Tandem synthesis of thiazolidine derivatives from primary amines, isothiocyanates, and bis(imidoyl) chlorides

2017 ◽  
Vol 14 (9) ◽  
pp. 1869-1874 ◽  
Author(s):  
Issa Yavari ◽  
Nooshin Zahedi ◽  
Stavroula Skoulika
2021 ◽  
Author(s):  
Jianguo Liu ◽  
Yanpei Song ◽  
Xiuzheng Zhuang ◽  
Mingyue Zhang ◽  
Longlong Ma

<p><a></a><a>The development of Earth-abundant reusable and no-toxic heterogeneous catalyst applied in the pharmaceutically, bio-active relevant compounds synthesis as well as other organic syntheses still remains as the most important goal of the general chemical research. N-methylated compounds, as one of the most essential bioactive compounds,</a> have been widely used in the fine and bulk industries for the production of high-value chemicals including pharmaceuticals, agrochemicals, and dyes. As their reports, activated toxic methyl iodide and dimethyl sulfoxide were usually employed in the traditional N-methylation, which easily suffer from narrow scopes of amines, generation of by-products, and a large amount of waste. <a>Very recently, </a>transition metal-catalyzed methylation of amines has become an efficient, practical, and cost-effective method for the one-pot selective synthesis of N-methylamines with C<sub>1</sub> sources. Herein, we first developed a simple and <a>environmentally friendly</a> method for the preparation of efficient, reusable, and low-cost graphene spheres encapsulated Ni/NiO nanoalloy catalysts (Ni/NiO@C) for highly selective synthesis of the N-methylated compounds by using various functional amines and aldehydes under easily handle-able and industrially <a></a><a>applicable </a>conditions.<b> </b>A large number of primary, secondary amines (more than 70 examples) could be converted smoothly to the corresponding N, N-dimethylamines with the participation of different functional aldehydes. The gram-scale synthesis was also demonstrated in an excellent yield; not only that, the catalyst was further proved that it could be easily recycled by its intrinsic magnetism and reused up to ten times without losing activity and selectivity. Both of them are the great advantages in contrast to other catalysts reported previously. And also, for the first time, we have developed the highly efficient, cost-effective tandem synthesis of N, N-dimethylamines products in a one-pot process by means of aldehydes and NH<sub>3</sub>. As far as we know, this is the first example of the synthesis of tertiary amines with the combined reaction process of reductive amination of aldehydes and N-methylation of primary amines only with the single one earth-abundant metal catalyst. Overall, the advantages of this newly developed method including operational simplicity, high stability, easily recyclable, cost-effective of the catalyst, and good functional group compatibility for the synthesis of N-methylation products, as well as the highly efficient and industrial applicable tandem synthesis process.</p>


2021 ◽  
Author(s):  
Jianguo Liu ◽  
Yanpei Song ◽  
Xiuzheng Zhuang ◽  
Mingyue Zhang ◽  
Longlong Ma

<p><a></a><a>The development of Earth-abundant reusable and no-toxic heterogeneous catalyst applied in the pharmaceutically, bio-active relevant compounds synthesis as well as other organic syntheses still remains as the most important goal of the general chemical research. N-methylated compounds, as one of the most essential bioactive compounds,</a> have been widely used in the fine and bulk industries for the production of high-value chemicals including pharmaceuticals, agrochemicals, and dyes. As their reports, activated toxic methyl iodide and dimethyl sulfoxide were usually employed in the traditional N-methylation, which easily suffer from narrow scopes of amines, generation of by-products, and a large amount of waste. <a>Very recently, </a>transition metal-catalyzed methylation of amines has become an efficient, practical, and cost-effective method for the one-pot selective synthesis of N-methylamines with C<sub>1</sub> sources. Herein, we first developed a simple and <a>environmentally friendly</a> method for the preparation of efficient, reusable, and low-cost graphene spheres encapsulated Ni/NiO nanoalloy catalysts (Ni/NiO@C) for highly selective synthesis of the N-methylated compounds by using various functional amines and aldehydes under easily handle-able and industrially <a></a><a>applicable </a>conditions.<b> </b>A large number of primary, secondary amines (more than 70 examples) could be converted smoothly to the corresponding N, N-dimethylamines with the participation of different functional aldehydes. The gram-scale synthesis was also demonstrated in an excellent yield; not only that, the catalyst was further proved that it could be easily recycled by its intrinsic magnetism and reused up to ten times without losing activity and selectivity. Both of them are the great advantages in contrast to other catalysts reported previously. And also, for the first time, we have developed the highly efficient, cost-effective tandem synthesis of N, N-dimethylamines products in a one-pot process by means of aldehydes and NH<sub>3</sub>. As far as we know, this is the first example of the synthesis of tertiary amines with the combined reaction process of reductive amination of aldehydes and N-methylation of primary amines only with the single one earth-abundant metal catalyst. Overall, the advantages of this newly developed method including operational simplicity, high stability, easily recyclable, cost-effective of the catalyst, and good functional group compatibility for the synthesis of N-methylation products, as well as the highly efficient and industrial applicable tandem synthesis process.</p>


1999 ◽  
Vol 8 (3) ◽  
pp. 241-246
Author(s):  
J. M. Forniés-Marquina ◽  
A. Siblini ◽  
L. Jorat ◽  
G. Noyel

2018 ◽  
Author(s):  
Diana Ainembabazi ◽  
Nan An ◽  
Jinesh Manayil ◽  
Kare Wilson ◽  
Adam Lee ◽  
...  

<div> <p>The synthesis, characterization, and activity of Pd-doped layered double hydroxides (Pd-LDHs) for for acceptorless amine dehydrogenation is reported. These multifunctional catalysts comprise Brønsted basic and Lewis acidic surface sites that stabilize Pd species in 0, 2+, and 4+ oxidation states. Pd speciation and corresponding cataytic performance is a strong function of metal loading. Excellent activity is observed for the oxidative transamination of primary amines and acceptorless dehydrogenation of secondary amines to secondary imines using a low Pd loading (0.5 mol%), without the need for oxidants. N-heterocycles, such as indoline, 1,2,3,4-tetrahydroquinoline, and piperidine, are dehydrogenated to the corresponding aromatics with high yields. The relative yields of secondary imines are proportional to the calculated free energy of reaction, while yields for oxidative amination correlate with the electrophilicity of primary imine intermediates. Reversible amine dehydrogenation and imine hydrogenation determine the relative imine:amine selectivity. Poisoning tests evidence that Pd-LDHs operate heterogeneously, with negligible metal leaching; catalysts can be regenerated by acid dissolution and re-precipitation.</p> </div> <br>


2018 ◽  
Vol 21 (4) ◽  
pp. 271-280 ◽  
Author(s):  
Mohammad A. Ghasemzadeh ◽  
Mohammad H. Abdollahi-Basir ◽  
Zahra Elyasi

Aim and Objective: The multi-component condensation of benzil, primary amines, ammonium acetate and various aldehydes was efficiently catalyzed using cobalt oxide nanoparticles under ultrasonic irradiation. This approach describes an effective and facile method for the synthesis of some novel 1,2,4,5-tetrasubstituted imidazole derivatives with several advantages such as high yields and short reaction times and reusability of the catalyst. Moreover, the prepared heterocyclic compounds showed high antibacterial activity against some pathogenic strains. Materials and Method: The facile and efficient approaches for the preparation of Co3O4 nanoparticles were carried out by one step method. The synthesized heterogeneous nanocatalyst was characterized by spectroscopic analysis including EDX, FE-SEM, VSM, XRD and FT-IR analysis. The as-synthesized cobalt oxide nanoparticles showed paramagnetic behaviour in magnetic field. In addition, the catalytic influence of the nanocatalyst was examined in the one-pot reaction of primary amines, benzil, ammonium acetate and diverse aromatic aldehydes under ultrasonic irradiation. All of the 1,2,4,5-tetrasubstituted imidazoles were investigated and checked with m.p., 1H NMR, 13C NMR and FT-IR spectroscopy techniques. The antibacterial properties of the heterocycles were evaluated in vitro by the disk diffusion against pathogenic strains such as Escherichia coli (EC), Bacillus subtillis (BS), Staphylococcus aureus (SA), Salmonellatyphi (ST) and Shigella dysentrae (SD) species. Results: In this research cobalt oxide nanostructure was used as a robust and green catalyst in the some novel imidazoles. The average particle size measured from the FE-SEM image is found to be 20-30 nm which confirmed to the obtained results from XRD pattern. Various electron-donating and electron-withdrawing aryl aldehydes were efficiently reacted in the presence of Co3O4 nanoparticles. The role of the catalyst as a Lewis acid is promoting the reactions with the increase in the electrophilicity of the carbonyl and double band groups. To investigate the reusability of the catalyst, the model study was repeated using recovered cobalt oxide nanoparticles. The results showed that the nanocatalyst could be reused for five times with a minimal loss of its activity. Conclusion: We have developed an efficient and environmentally friendly method for the synthesis of some tetrasubstituted imidazoles via three-component reaction of benzil, primary amines, ammonium acetate and various aldehydes using Co3O4 NPs. The present approach suggests different benefits such as: excellent yields, short reaction times, simple workup procedure and recyclability of the magnetic nanocatalyst. The prepared 1,2,4,5-tetrasubstituted imidazoles revealed high antibacterial activities and can be useful in many biomedical applications.


2020 ◽  
Vol 7 (2) ◽  
pp. 226-238
Author(s):  
Petro P. Ony`sko ◽  
Tetyana I. Chudakova ◽  
Vladimir V. Pirozhenko ◽  
Alexandr B. Rozhenko

The potentialities of condensation of α-ketophosphonates with primary amines for direct synthesis of α-iminophosphonates have been revealed. Diesters of α-ketophosphonic acids react with the primary amines by two competitive pathways: with a formation of α-iminophosphonates or a C-P bond cleavage resulting in a hydrogen phosphonate and an acylated amine. In many cases, the latter undesirable pathway is dominant, especially for more nucleophilic alkyl amines. Using metallic salts of α-ketophosphonates avoids the C-P bond cleavage, allowing direct preparation of α-phosphorylated imines by the reaction with primary amines. This strategy provides an atom economy single-stage synthesis of iminophosphonates – precursors of bio relevant phosphorus analogs of α-amino acids. Methyl sodium iminophosphonates, bearing aryl or heteryl substituents at the imino carbon atom exist in solutions at room temperature as an equilibrium mixture of Z- and E-isomers. A configuration of the C=N bond can be controlled by the solvent: changing the aprotic dipolar solvent DMSO-d6 by water or alcohols leads to the change from a predominant Z-isomer to almost an exclusive E-form. In contrast, diesters of the respective iminophosphonates exist in non-protic solvents predominantly in Econfiguration. The solvent effect on E-Z stereochemistry is demonstrated by DFT calculations.


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